Canonical Allele Identifier: CA1037173518
Gene: LRP1B HGNC NCBI

Linked Data

dbSNP Id: rs1696102541

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.140963525_140963527del , CM000664.2:g.140963525_140963527del GRCh38
NC_000002.11:g.141721094_141721096del , CM000664.1:g.141721094_141721096del GRCh37
NC_000002.10:g.141437564_141437566del NCBI36
NG_051023.1:g.1173939_1173941del

Transcript Alleles

HGVS Amino-acid change
ENST00000389484.8:c.2888-11585_2888-11583del MANE Select ENSP00000374135.3:n.2888-11585_2888-11583...
ENST00000389484.7:c.2888-11585_2888-11583del ENSP00000374135.3:n.2888-11585_2888-11583...
ENST00000434794.1:c.323-11585_323-11583del ENSP00000413239.1:n.323-11585_323-11583de...
ENST00000618808.4:c.2546-11585_2546-11583del ENSP00000478868.1:n.2546-11585_2546-11583...
NM_018557.2:c.2888-11585_2888-11583del NP_061027.2:n.2888-11585_2888-11583del
XM_011511352.1:c.2999-11585_2999-11583del XP_011509654.1:n.2999-11585_2999-11583del...
XM_017004341.1:c.2498-11585_2498-11583del XP_016859830.1:n.2498-11585_2498-11583del...
XR_001738778.1:n.4622-11585_4622-11583del
NM_018557.3:c.2888-11585_2888-11583del MANE Select NP_061027.2:n.2888-11585_2888-11583del